Key result
UV/Visible spectroscopy performs robustly versus ELISA for quantifying bovine serum albumin and creatinine.
Why the study?
The albumin/creatinine ratio is essential for monitoring diabetic kidney disease and associated cardiovascular risk, motivating the development of rapid, cost-effective point-of-care quantification methods.
Does UV/Visible spectroscopy accurately quantify urinary albumin and creatinine compared to ELISA in spiked aqueous urine samples?
Does UV/Visible spectroscopy accurately quantify urinary albumin and creatinine compared to ELISA in spiked aqueous urine samples?
Effect estimate: R2PRED 0.96 (BSA), 0.95 (creatinine)
This is the authors' abstract. We don't add key points for this paper.
Albuminuria is a sensitive biomarker of kidney dysfunction, and the albumin/creatinine ratio (ACR) is an essential measure for monitoring diabetic kidney disease (DKD). Abnormal levels can indicate a propensity for progressive renal failure and other complications such as cardiovascular diseases. This study employed UV/Visible spectroscopy to analyze aqueous urine samples spiked with bovine serum albumin (BSA) and creatinine at clinically relevant concentrations (0–30 mg/L for albumin and 600–1800 mg/L for creatinine) using a multivariate method. UV/Visible spectra of co-spiked samples recorded in triplicate revealed distinct bands at 229 nm and 249 nm, corresponding to BSA and creatinine, respectively, alongside other amino acid bands. Partial Least Squares Regression (PLS-R) analysis for BSA yielded a Root Mean Square Error of Calibration (RMSEC) and Cross-Validation (RMSECV) values of 66.93 and 73.92 mg/L, respectively. For creatinine, RMSEC and RMSECV values were 244.32 and 275.65 mg/L, respectively. Prediction models for both BSA and creatinine compared to ELISA demonstrated a robust performance with R2PRED values of 0.96 and 0.95, respectively, indicating strong model reliability. The Limit of Detection (LOD) for co-spiked samples was 19.82 mg/L for BSA and 58.43 mg/L for creatinine. The significance of the achieved Limit of Detection (LOD) lies in its ability to measure concentrations well below the normal physiological ranges of 0–30 mg/L for albumin and 600–1800 mg/L for creatinine. These results demonstrate the proof of concept of applying an UV/Visible-spectroscopy-based method as a rapid, cost-effective point-of-care (PoC) tool for ACR measurements, offering promising applications in the early diagnosis, monitoring, and prognosis of diabetic kidney disease and associated cardiovascular complications. The next stage will involve a pilot trial to evaluate the technology’s potential using clinical patients.
UV/Visible spectroscopy demonstrates proof-of-concept as a rapid, cost-effective point-of-care tool for quantifying urinary albumin and creatinine.
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Dias et al. (2025) studied Albuminuria / Diabetic kidney disease. UV/Visible spectroscopy vs. ELISA was evaluated on Prediction models for BSA and creatinine compared to ELISA (R2PRED 0.96 (BSA), 0.95 (creatinine)). UV/Visible spectroscopy demonstrated robust performance for quantifying bovine serum albumin and creatinine compared to ELISA, with R2PRED values of 0.96 and 0.95, respectively.
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